chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185870788058707881CT18GENIChomozygous46665542
185871143758711438TTA16GENICpossibly homozygous46665543
185871229458712295CT15GENIChomozygous46612027
185871288858712889AT28GENIChomozygous46612028
185871299658712997TC10GENICpossibly homozygous46612029
185871342558713426A-12GENIChomozygous46612030